File:Autosomal_recessive_-_en.svg
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Summary
DescriptionAutosomal recessive - en.svg |
English: Autosomal recessive inheritance (English version)
Español: Herencia autosómica recesiva (versión en Español)
Türkçe: Otomozal resesif kalıtsallık (Türkçe versiyon) |
Date | |
Source | |
Author | Domaina, Kashmiri and SUM1 |
Other versions |
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Licensing
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Items portrayed in this file
depicts
20 January 2020
image/svg+xml
2db88f1617cd4a7e4cd7d1adac624d2a645dae02
28,487 byte
1,283 pixel
738 pixel
File history
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Date/Time | Thumbnail | Dimensions | User | Comment | |
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current | 22:38, 5 October 2023 | 738 × 1,283 (29 KB) | Andreyyshore | attempting to fix font size and spacing for newly-added languages | |
22:34, 5 October 2023 | 738 × 1,283 (29 KB) | Andreyyshore | added Romanian and Turkish translations | ||
02:15, 15 August 2023 | 738 × 1,283 (28 KB) | Parzeus | File uploaded using svgtranslate tool (https://svgtranslate.toolforge.org/). Added translation for pt-br. | ||
12:18, 21 May 2023 | 738 × 1,283 (26 KB) | Kashmiri | Title in sans-serif, too | ||
12:16, 21 May 2023 | 738 × 1,283 (26 KB) | Kashmiri | Code optimised | ||
12:41, 25 October 2020 | 738 × 1,283 (27 KB) | Kashmiri | Further code cleanup | ||
12:18, 25 October 2020 | 738 × 1,283 (27 KB) | Kashmiri | Code cleanup and optimisation. Replacing Arial typeface with generic (sans-serif) typeface for better display cross-OS. | ||
03:47, 21 January 2020 | 738 × 1,283 (79 KB) | SUM1 | Further non-sex-linkage fix and fixed arrows | ||
03:30, 21 January 2020 | 738 × 1,283 (79 KB) | SUM1 | Horizontally aligned child text | ||
22:55, 20 January 2020 | 738 × 1,283 (79 KB) | SUM1 | Centred child text |
File usage
More than 100 pages use this file. The following list shows the first 100 pages that use this file only. A full list is available.
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- 6-Pyruvoyltetrahydropterin synthase deficiency
- AREDYLD syndrome
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- Abdallat–Davis–Farrage syndrome
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- Ackerman syndrome
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- Adenosine deaminase deficiency
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- Analbuminaemia
- Aspartylglucosaminuria
- Asplenia with cardiovascular anomalies
- Autosomal recessive multiple epiphyseal dysplasia
- Bangstad syndrome
- Bardet–Biedl syndrome
- Bare lymphocyte syndrome
- Bare lymphocyte syndrome type II
- Bernard–Soulier syndrome
- Blount's disease
- Buphthalmos
- Carbamoyl phosphate synthetase I deficiency
- Cenani–Lenz syndactylism
- Cerebral palsy
- Cerebrotendineous xanthomatosis
- Chorea-acanthocytosis
- Chédiak–Higashi syndrome
- Cohen syndrome
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- Costeff syndrome
- Cutis marmorata telangiectatica congenita
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- Fukuyama congenital muscular dystrophy
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- Galactose epimerase deficiency
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- Glanzmann's thrombasthenia
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- Glycogen storage disease type V
- Gray platelet syndrome
- Gunther disease
- Hereditary pyropoikilocytosis
- Hermansky–Pudlak syndrome
- Hyperlysinemia
- Hypoprothrombinemia
- Immunodeficiency–centromeric instability–facial anomalies syndrome
- Joubert syndrome
- Krabbe disease
- Laurence–Moon syndrome
- Leigh syndrome
- Letterer–Siwe disease
- Leukocyte adhesion deficiency
- Lipoid congenital adrenal hyperplasia
- Lipoprotein lipase deficiency
- Majewski's polydactyly syndrome
- Malonic aciduria
- Maple syrup urine disease
- Mediastinal fibrosis
- Medium-chain acyl-coenzyme A dehydrogenase deficiency
- Metachromatic leukodystrophy
- Metaphyseal dysplasia
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- Mulibrey nanism
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- Nijmegen breakage syndrome
- Oguchi disease
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- Peters-plus syndrome
- Prolidase deficiency
- Pseudo-Hurler polydystrophy
- Purine nucleoside phosphorylase deficiency
- Raine syndrome
- Rosselli–Gulienetti syndrome
- Rotor syndrome
- Sabinas brittle hair syndrome
- Salla disease
- Sandhoff disease
- Sarcosinemia
- Severe congenital neutropenia
- Short-chain acyl-coenzyme A dehydrogenase deficiency
- Sitosterolemia
- Spinal muscular atrophy
- Thrombotic thrombocytopenic purpura
- Thyroid dyshormonogenesis
- Triosephosphate isomerase deficiency
- Urofacial syndrome
- Usher syndrome
- Waardenburg syndrome
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Global file usage
The following other wikis use this file:
- Usage on ar.wikipedia.org
- Usage on az.wikipedia.org
- Usage on bn.wikipedia.org
- Usage on bs.wikipedia.org
- Bardet–Biedlov sindrom
- Mišićna distrofija udovi-pojas
- MOPD II
- Frank–Ter Haarov sindrom
- Pravi hermafroditizam
- Nedostatak 5α-reduktaze
- Waardenburgov sindrom
- Nedostatak leukocitne adhezije
- Nedostatak adenozin-deaminaze
- Galaktozialidoza
- Nedostatak prolidaze
- Sindrom HUPRA
- Krvni antigen Vel
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- Bruckov sindrom
- Usherov sindrom
- Nedostatak srednjelančane acil-koenzim A dehidrogenaze
- Alströmov sindrom
- Primarna hiperoksalurija
- Sensenbrennerin sindrom
- Sitosterolemija
- Leukoencefalopatija sa nestajanjem bijele mase
- Spinalna mišićna atrofija
- Zellwegerov sindrom
- Usage on cs.wikipedia.org
- Usage on el.wikipedia.org
- Usage on en.wikibooks.org
- Usage on es.wikipedia.org
- Usage on fa.wikipedia.org
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Metadata
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Width | 738 |
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Height | 1283 |
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